CHEBI:59973 - 1-(L-norleucin-6-yl)pyrraline

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 1-(L-norleucin-6-yl)pyrraline
ChEBI ID CHEBI:59973
ChEBI ASCII Name 1-(L-norleucin-6-yl)pyrraline
Definition An N-substituted pyrraline formed via Maillard reaction of L-lysine with glucose.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C12H18N2O4
Net Charge 0
Average Mass 254.28230
Monoisotopic Mass 254.12666
InChI InChI=1S/C12H18N2O4/c13-11(12(17)18)3-1-2-6-14-9(7-15)4-5-10(14)8-16/h4-5,7,11,16H,1-3,6,8,13H2,(H,17,18)/t11-/m0/s1
InChIKey VTYFITADLSVOAS-NSHDSACASA-N
SMILES N[C@@H](CCCCn1c(CO)ccc1C=O)C(O)=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-(L-norleucin-6-yl)pyrraline (CHEBI:59973) is a N-substituted pyrraline (CHEBI:131546)
1-(L-norleucin-6-yl)pyrraline (CHEBI:59973) is a L-lysine derivative (CHEBI:25095)
1-(L-norleucin-6-yl)pyrraline (CHEBI:59973) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
IUPAC Name
6-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]-L-norleucine
Synonyms Sources
(S)-α-amino-2-formyl-5-(hydroxymethyl)-1H-pyrrole-1-hexanoic acid ChemIDplus
2-Amino-6-(2-formyl-5-hydroxymethylpyrrol-1-yl)hexanoic acid ChemIDplus
2-Fhmpn ChemIDplus
2-Formyl-5-(hydroxymethyl)pyrrole-1-norleucine ChemIDplus
ε-[2-formyl-5-(hydroxymethyl)pyrrole-1-yl]-L-norleucine ChEBI
ε-L-lysyl pyrraline ChEBI
ε-L-lysylpyrraline ChEBI
ε-lysylpyrraline ChEBI
ε-pyrraline ChEBI
L-lysyl pyrraline ChEBI
Pyrraline ChemIDplus
pyrraline-lysine ChEBI
Registry Numbers Types Sources
7096285 Beilstein Registry Number Beilstein
7096285 Reaxys Registry Number Reaxys
74509-14-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
1556177 PubMed citation Europe PMC
2715232 PubMed citation Europe PMC
2917974 PubMed citation Europe PMC
Last Modified
23 August 2017